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Colin Wallis

Showing results (51-60 of 63) with videos related to

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Chest|May 11, 2020
Cardiorespiratory Progression Over 5 Years and Role of Corticosteroids in Duchenne Muscular Dystrophy: A Single-Site Retrospective Longitudinal StudyFederica Trucco, Joana P Domingos, Chee Geap Tay, et al.
The European Respiratory Journal|November 11, 2017
Pulmonary function deficits in newborn screened infants with cystic fibrosis managed with standard UK care are mild and transientGwyneth Davies, Janet Stocks, Lena P Thia, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 12, 2020
Minimal change in structural, functional and inflammatory markers of lung disease in newborn screened infants with cystic fibrosis at one yearGwyneth Davies, Lena P Thia, Janet Stocks, et al.
Thorax|July 4, 2012
Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screeningAh-Fong Hoo, Lena P Thia, The Thanh Diem Nguyen, et al.
The European Respiratory Journal|July 20, 2019
ERS statement on tracheomalacia and bronchomalacia in childrenColin Wallis, Efthymia Alexopoulou, Juan L Antón-Pacheco, et al.
Muscle & Nerve|October 4, 2021
Genotype-related respiratory progression in Duchenne muscular dystrophy-A multicenter international studyFederica Trucco, Deborah Ridout, Joana Domingos, et al.
Stem Cells Translational Medicine|May 26, 2017
Tracheal Replacement Therapy with a Stem Cell-Seeded Graft: Lessons from Compassionate Use Application of a GMP-Compliant Tissue-Engineered MedicineMartin J Elliott, Colin R Butler, Aikaterini Varanou-Jenkins, et al.
Pediatric Pulmonology|July 28, 2023
Unsupervised home spirometry is not equivalent to supervised clinic spirometry in children and young people with cystic fibrosis: Results from the CLIMB-CF studyClaire Edmondson, Nicole Westrupp, Christopher Short, et al.
American Journal of Medical Genetics. Part A|March 15, 2016
Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findingsMadeleine Tooley, Danielle Lynch, Francois Bernier, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalitiesVictoria H Castleman, Leila Romio, Rahul Chodhari, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Chest|May 11, 2020
Cardiorespiratory Progression Over 5 Years and Role of Corticosteroids in Duchenne Muscular Dystrophy: A Single-Site Retrospective Longitudinal StudyFederica Trucco, Joana P Domingos, Chee Geap Tay, et al.
The European Respiratory Journal|November 11, 2017
Pulmonary function deficits in newborn screened infants with cystic fibrosis managed with standard UK care are mild and transientGwyneth Davies, Janet Stocks, Lena P Thia, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 12, 2020
Minimal change in structural, functional and inflammatory markers of lung disease in newborn screened infants with cystic fibrosis at one yearGwyneth Davies, Lena P Thia, Janet Stocks, et al.
Thorax|July 4, 2012
Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screeningAh-Fong Hoo, Lena P Thia, The Thanh Diem Nguyen, et al.
The European Respiratory Journal|July 20, 2019
ERS statement on tracheomalacia and bronchomalacia in childrenColin Wallis, Efthymia Alexopoulou, Juan L Antón-Pacheco, et al.
Muscle & Nerve|October 4, 2021
Genotype-related respiratory progression in Duchenne muscular dystrophy-A multicenter international studyFederica Trucco, Deborah Ridout, Joana Domingos, et al.
Stem Cells Translational Medicine|May 26, 2017
Tracheal Replacement Therapy with a Stem Cell-Seeded Graft: Lessons from Compassionate Use Application of a GMP-Compliant Tissue-Engineered MedicineMartin J Elliott, Colin R Butler, Aikaterini Varanou-Jenkins, et al.
Pediatric Pulmonology|July 28, 2023
Unsupervised home spirometry is not equivalent to supervised clinic spirometry in children and young people with cystic fibrosis: Results from the CLIMB-CF studyClaire Edmondson, Nicole Westrupp, Christopher Short, et al.
American Journal of Medical Genetics. Part A|March 15, 2016
Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findingsMadeleine Tooley, Danielle Lynch, Francois Bernier, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalitiesVictoria H Castleman, Leila Romio, Rahul Chodhari, et al.
Pageof 7